HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795793Generated: October 26, 2026
1,2-Dichlorobenzene → Benzyl 2-[3,5-dichloro-2-methyl-6-oxo-1(6H)-pyrazinyl]acetate
https://huagongshe.com/reaction/1795793
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichlorobenzene | HCID 7239 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Benzyl-N-(1-cyanoethyl)glycine hydrochloride | HCID 68560147 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Benzyl 2-[3,5-dichloro-2-methyl-6-oxo-1(6H)-pyrazinyl]acetate | HCID 10663926 | 55% |
Reaction Steps
A stirred mixture of oxalyl chloride (5.3 mL, 60 mmol) and benzyl-N-(1-cyanoethyl)glycine hydrochloride (3.82 g, 15 mmol), as prepared in the preceding step, in 1,2-dichlorobenzene (30 mL) was heated to 100° C. overnight. The solvent was evaporated in vacuo and the residue was purified by flash column chromatography to give a solid. 10% Ethyl acetate in hexane (100 mL) was added and the solid was collected to give the title compound as an orange crystalline solid (2.7 g, 55%). 1H NMR (CDCl3) δ 7.38 (m, 5 H), 5.24 (s, 2 H), 4.89 (s, 2 H), 2.34 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030110B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-3561f8615a3a4d75897ec82536a6995b |
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| Source note | uspto-grants-2006_04 |
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